Recherche de Sous-structure

7222

CCOC(=O)c1ccc(NC(O)=[SH]CCCN2CCN(Cc3ccc(Cl)cc3)CC2)cc1.Cl.Cl
Reaction #3902
N-(4-ethoxycarbonylphenyl)-S-{3-[4-(4-chlorobenzyl)piperazin-1-yl]propyl}thiocarbamate dihydrochloride
Rendement 55.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(NC(=O)Nc2ccc(Cl)c(C(F)(F)F)c2)cc1
Reaction #165512
N-(4-chloro-3-(trifluoromethyl)phenyl)-N′-(4-ethoxycarbonylphenyl)urea
Rendement 97.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)COC(=O)c1ccc(NC(=O)OCCO)cc1
Reaction #204362
DOI: 10.1039/C8SC04228D
CCOC(=O)c1ccc(NC(=O)Nc2ccc(Cl)c(C(F)(F)F)c2)cc1
Reaction #221731
DOI: 10.1039/C8SC04228D
CCOC(=O)c1ccc(NC(=O)Nc2cccc(-c3c(C(=O)c4ccccc4)cnc4c(C(F)(F)F)cccc34)c2)cc1
Reaction #275997
DOI: 10.1039/C8SC04228D
CCOC(=O)C1=C(Nc2ccc(C(=O)OCC)cc2)OCC1=O
Reaction #318307
Ethyl 2-[[4-(ethoxycarbonyl)phenyl]amino]4,5-dihydro-4-oxo-3-furancarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(NC(=O)NC2CCC2)cc1
Reaction #370793
DOI: 10.1039/C8SC04228D
CC(C)OC(=O)c1ccc(N=C=O)cc1
Reaction #378101
DOI: 10.1039/C8SC04228D
CCOC(=O)c1ccc(NC(=O)NC2CCC2)cc1
Reaction #496027
title compound
Rendement 88.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(NC(=O)NCC2CC2)cc1
Reaction #496043
title compound
Rendement 107.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(NC(=O)OCc2cn(-c3cc4cc(C(=O)OCC)c(=O)[nH]c4cc3C(F)(F)F)cn2)cc1
Reaction #499252
title compound
Rendement 98.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(NC(=O)NCc2ccn(-c3cc4cc(C(=O)OCC)c(=O)[nH]c4cc3C(F)(F)F)c2)cc1
Reaction #499254
title compound
Rendement 60.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(NC(=O)N2CCC3(CC2)CN(S(C)(=O)=O)c2ccccc23)cc1
Reaction #515763
1500
Rendement 100.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(NC(=O)Nc2ccc(Cl)c(C(F)(F)F)c2)cc1
Reaction #578274
N-(4-chloro-3-(trifluoromethyl)phenyl)-N′-(4-ethoxycarbonylphenyl) urea
Rendement 97.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(NC(=O)NCC2CC2)cc1
Reaction #602506
title compound
Rendement 107.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(NC(=O)Nc2ccc(Br)cc2F)cc1
Reaction #604606
title compound
Rendement 70.6%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(NC(=O)NCCCN2CCN(Cc3ccc(Cl)cc3)CC2)cc1.Cl
Reaction #630355
title compound
Rendement 62.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(NC(=O)N2CCC3(CC2)CN(S(C)(=O)=O)c2ccccc23)cc1
Reaction #723083
1500
Rendement 100.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(NC(=O)NCC2CC(OC)OC2OC)cc1
Reaction #738080
crude product
Rendement 104.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(N=C=O)ccc1C(=O)OC(C)(C)C
Reaction #752158
DOI: 10.1039/C8SC04228D
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